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Duodenoscope - Argentina Medical Device Registration

Access comprehensive regulatory information for Duodenoscope in the Argentina medical device market through Pure Global AI's free database. This Class I-II Registration Modification medical device is registered with Argentina's ANMAT (National Administration of Drugs, Food and Medical Technology). The device was registered on April 29, 2024.

This page provides complete registration details including product code (340-206), brand name (Ambu), authorized representative information, registration type, and regulatory compliance data from the official Argentina ANMAT medical device database. Pure Global AI offers free access to Argentina's medical device registry, helping global MedTech companies navigate Argentina regulations efficiently.

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Argentina ANMAT Data
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Class I-II Registration Modification
Duodenoscope
Duodenoscopio
Argentina Medical Device Registration
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Product Information

aScope Duodenum aBox Duodenum

Spanish:

aScope Duodeno aBox Duodeno

Device Classification
Registration Type
Class I-II Registration Modification
Modificaciรณn de Registro Clase I-II
Product Code
340-206
Brand Name
Ambu
Product Name
Duodenoscope
Duodenoscopio
Registration Information
Registration Date
April 29, 2024
Database ID
cmhayu0e30ex9ekuz8psoojvu
Authorized Representative